Early Time Courses of Recurrent Venous Thromboembolism and Bleeding during Apixaban or Dalteparin Therapy for Patients with Cancer

被引:4
|
作者
Cohen, Alexander T. [1 ]
Creeper, Katherine J. [1 ,2 ,3 ,13 ]
Alikhan, Raza [4 ]
Er, Chaozer [5 ]
Connors, Jean M. [6 ]
Huisman, Menno V. [7 ]
Munoz, Andres [8 ]
Vescovo, Giorgio [9 ]
Bauersachs, Rupert [10 ,11 ]
Ageno, Walter [12 ]
Agnelli, Giancarlo [9 ]
Becattini, Cecilia [9 ]
机构
[1] Guys & St Thomas NHS Fdn Trust, Dept Haemostasis & Thrombosis, London, England
[2] Sir Charles Gairdner Hosp, Haematol Dept, Perth, Australia
[3] PathWest Lab Med, Haematol Dept, Nedlands, Australia
[4] Univ Hosp Wales, Haematol Dept, Cardiff, Wales
[5] Woodlands Hlth, Dept Gen Med, Singapore, Singapore
[6] Brigham & Womens Hosp, Heart & Vasc Ctr, Boston, MA USA
[7] Leiden Univ, Med Ctr, Leiden & Dutch Thrombosis Network, Dept Med Thrombosis & Hemostasis, Leiden, Netherlands
[8] Univ Complutense Madrid, Gregorio Maranon Hlth Res Inst, Dept Med Oncol, Madrid, Spain
[9] Osped St Antonio, Dept Internal Med, Padua, Italy
[10] Cardioangiol Ctr Bethanien CCB, Frankfurt, Germany
[11] Johannes Gutenberg Univ Mainz, Ctr Thrombosis & Hemostasis, Mainz, Germany
[12] Univ Insubria, Dipartimento Med & Chirurg, Varese, Italy
[13] POB 306, Floreat, WA 6014, Australia
关键词
anticoagulants; bleeding; cancer; dalteparin; thrombosis;
D O I
10.1055/s-0043-1778642
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background In patients with acute venous thromboembolism (VTE), the rates of recurrence and major bleeding are highest during the first weeks of anticoagulation. The CARAVAGGIO trial demonstrated noninferiority of apixaban to dalteparin for treatment of cancer-associated VTE without an increased risk of major bleeding. We compared the early time course of VTE recurrence and major bleeding events of apixaban compared with dalteparin at 7, 30, and 90 days of treatment in patients with cancer-associated VTE. Methods The study design of the CARAVAGGIO trial has been described. Eligible patients were randomly assigned to receive monotherapy with either apixaban or dalteparin for 6 months. The primary efficacy outcome was the incidence of objectively confirmed recurrent VTE. The primary safety outcome was major bleeding. Results In 1,155 patients, recurrent VTE after 7, 30, and 90 days occurred in 6 (1%), 15 (2.6%), and 27 (4.7%) patients in the apixaban arm versus 5 (0.9%), 20 (3.5%), and 36 (6.2%) patients respectively in the dalteparin arm. By day 7, 30, and 90, major bleeding events had occurred in 3 (0.5%), 9 (1.6%), and 16 (2.8%) patients in the apixaban group versus 5 (0.9%), 11 (1.9%), and 17 (2.9%) patients in the dalteparin group. Conclusion The frequencies of recurrent VTE and major bleeding events at 7, 30, and 90 days of apixaban compared with dalteparin were similar in patients with cancer-associated VTE. This supports the use of apixaban for the initiation and early phase of anticoagulant therapy in cancer-associated VTE.
引用
收藏
页码:676 / 683
页数:8
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